TruVision Health LLC

Recall #F-0942-2023 · Initiated 2023-04-27

Plain-language summary

by FoodRecallsDB.info

What happened

TruVision Health LLC is recalling their reFORM dietary supplement because it contains DMHA and/or hordenine, ingredients that the FDA determined are not safe for use in dietary supplements. About 2,535 packs of this product were distributed across the U.S. and several other countries.

Who is at risk

Anyone who purchased and is using this product should be concerned, as these ingredients may pose health risks.

What to do

Stop using reFORM immediately if you have it. Contact TruVision Health LLC or check the FDA website for instructions on how to return or dispose of the product safely. If you experience any health problems after using this product, contact your doctor or poison control.

Product

reFORM

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

Quantity affected

2,535 packs

Distribution

Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand

Lot / code info

Lot 34159

Voluntary / mandated

Voluntary: Firm initiated

Initial notification

Press Release